雷布
肽
计算生物学
抗毒素
生物
噬菌体展示
合理设计
生物化学
化学
表位
细胞生物学
合成生物学
肽序列
肽库
抗菌肽
血浆蛋白结合
细菌
蛋白质-蛋白质相互作用
原噬菌体
蛋白质工程
作者
Dia A. Ghose,Sebastian Swanson,Foster Birnbaum,Dustin Britton,Jessie L. Gan,Emily M. Mahoney,Michael T. Laub,Amy E. Keating
标识
DOI:10.1021/acssynbio.5c00498
摘要
Toxin-antitoxin (TA) systems are widespread antiphage defense elements in bacteria that may impede successful phage therapy. Phage-encoded inhibitors of these systems have been discovered that enhance phage infection capacity. We used fragment-based design with deep-learning scoring functions to design peptide inhibitors of the toxin RelE. Our peptides extend a fragment of the native RelB antitoxin and are sufficient to inhibit RelE toxicity. Successful inhibitors share a highly conserved binding mode that mimics the native antitoxin but have diverse sequences, with alternative contacts used to form the peptide-protein interface. Designed peptides show different interaction specificities toward RelE family proteins, distinct from the wild-type RelB antitoxin, and inhibit the antiphage defense activity of multiple orthologous RelBE systems. This work showcases the use of structure-based computational design to generate peptide binders that serve as potential counter-defense elements.
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